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T8766

Sigma-Aldrich

p-Toluidine

powder

Synonym(s):

4-Aminotoluene, 4-Methylaniline

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About This Item

Linear Formula:
CH3C6H4NH2
CAS Number:
106-49-0
Molecular Weight:
107.15
Beilstein/REAXYS Number:
471281
EC Number:
203-403-1
MDL number:
MFCD00007906
UNSPSC Code:
12352100

vapor density

3.9 (vs air)

form

powder

autoignition temp.

899 °F

expl. lim.

6.6 %

color

tan to brown

bp

200 °C (lit.)

mp

41-46 °C (lit.)

density

0.973 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

Cc1ccc(N)cc1

InChI

1S/C7H9N/c1-6-2-4-7(8)5-3-6/h2-5H,8H2,1H3

InChI key

RZXMPPFPUUCRFN-UHFFFAOYSA-N

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replaced by

Product No.
Description
Pricing

461121

p-Toluidine, 99%

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Carc. 2 - Eye Irrit. 2 - Skin Sens. 1A

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

188.6 °F - closed cup

flash_point_c

87 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
087K3740
057K3528
057H3462
028H3439
086K3708

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Paul G Stevenson et al.
Journal of chromatography. A, 1218(45), 8255-8263 (2011-10-11)
Several simple techniques are presented for the identification of the boundaries of chromatographic peaks. These methods provide a significant reduction in the time needed to perform the rapid, automatic calculation of the central peak moments and to evaluate the quality
Mutagenic potential of some chemical components of dental materials.
E G Miller et al.
Dental materials : official publication of the Academy of Dental Materials, 2(4), 163-165 (1986-08-01)
Shunji Ito et al.
The Journal of organic chemistry, 70(6), 2285-2293 (2005-03-12)
[reaction: see text] N,N-Di(6-azulenyl)-p-toluidine (1a) and N,N,N',N'-tetra(6-azulenyl)-p-phenylenediamine (2a) and their derivatives with 1,3-bis(ethoxycarbonyl) substituents on each 6-azulenyl group (1b and 2b) were prepared by Pd-catalyzed amine azulenylation and characterized as a study into new aromatic amines for multistage amphoteric redox
D R Doerge et al.
Chemical research in toxicology, 4(5), 556-560 (1991-09-01)
The metabolism of three arylamine substrates by H2O2 in the presence of each of the peroxidative enzymes chloroperoxidase (CPX) and pea seed peroxygenase (PSM) was conducted with normal H2O2 and with 18O-labeled H2O2. The resulting C-nitroso aromatic metabolites were examined
G Wolf et al.
Biotechnology and bioengineering, 72(3), 297-306 (2001-01-03)
The use of two-dimensional scanning fluorometry as an on-line, noninvasive, in situ bioreactor monitoring technique is extended to complex bioprocesses using mixed cultures, with particular attention to biofilm systems. Using the example of spectra subtraction, it is demonstrated that established
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